IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma

Abstract Background Asthma was identified as the most common comorbidity in hospitalized patients during the 2009 H1N1 influenza pandemic. We determined using a murine model of allergic asthma whether these mice experienced increased morbidity from pandemic H1N1 (pH1N1) viral infection and whether b...

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Main Authors: Kimia Shahangian, David A. Ngan, H. H. Rachel Chen, Yeni Oh, Anthony Tam, Jing Wen, Chung Cheung, Darryl A. Knight, Delbert R. Dorscheid, Tillie L. Hackett, Michael R. Hughes, Kelly M. McNagny, Jeremy A. Hirota, Masahiro Niikura, S. F. Paul Man, Don D. Sin
Format: Article
Language:English
Published: BMC 2021-03-01
Series:Respiratory Research
Online Access:https://doi.org/10.1186/s12931-021-01669-0
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spelling doaj-7e4c9487ca8144e18fc0c72a35f4c5812021-03-11T11:41:53ZengBMCRespiratory Research1465-993X2021-03-0122111110.1186/s12931-021-01669-0IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthmaKimia Shahangian0David A. Ngan1H. H. Rachel Chen2Yeni Oh3Anthony Tam4Jing Wen5Chung Cheung6Darryl A. Knight7Delbert R. Dorscheid8Tillie L. Hackett9Michael R. Hughes10Kelly M. McNagny11Jeremy A. Hirota12Masahiro Niikura13S. F. Paul Man14Don D. Sin15Centre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaDepartment of Medicine, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaDepartment of Health Sciences, Simon Fraser UniversityCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaCentre for Heart Lung Innovation, St. Paul’s Hospital, University of British ColumbiaAbstract Background Asthma was identified as the most common comorbidity in hospitalized patients during the 2009 H1N1 influenza pandemic. We determined using a murine model of allergic asthma whether these mice experienced increased morbidity from pandemic H1N1 (pH1N1) viral infection and whether blockade of interleukin-4 receptor α (IL-4Rα), a critical mediator of Th2 signalling, improved their outcomes. Methods Male BALB/c mice were intranasally sensitized with house dust mite antigen (Der p 1) for 2 weeks; the mice were then inoculated intranasally with a single dose of pandemic H1N1 (pH1N1). The mice were administered intraperitoneally anti-IL-4Rα through either a prophylactic or a therapeutic treatment strategy. Results Infection with pH1N1 of mice sensitized to house dust mite (HDM) led to a 24% loss in weight by day 7 of infection (versus 14% in non-sensitized mice; p < .05). This was accompanied by increased viral load in the airways and a dampened anti-viral host responses to the infection. Treatment of HDM sensitized mice with a monoclonal antibody against IL-4Rα prior to or following pH1N1 infection prevented the excess weight loss, reduced the viral load in the lungs and ameliorated airway eosinophilia and systemic inflammation related to the pH1N1 infection. Conclusion Together, these data implicate allergic asthma as a significant risk factor for H1N1-related morbidity and reveal a potential therapeutic role for IL-4Rα signalling blockade in reducing the severity of influenza infection in those with allergic airway disease.https://doi.org/10.1186/s12931-021-01669-0
collection DOAJ
language English
format Article
sources DOAJ
author Kimia Shahangian
David A. Ngan
H. H. Rachel Chen
Yeni Oh
Anthony Tam
Jing Wen
Chung Cheung
Darryl A. Knight
Delbert R. Dorscheid
Tillie L. Hackett
Michael R. Hughes
Kelly M. McNagny
Jeremy A. Hirota
Masahiro Niikura
S. F. Paul Man
Don D. Sin
spellingShingle Kimia Shahangian
David A. Ngan
H. H. Rachel Chen
Yeni Oh
Anthony Tam
Jing Wen
Chung Cheung
Darryl A. Knight
Delbert R. Dorscheid
Tillie L. Hackett
Michael R. Hughes
Kelly M. McNagny
Jeremy A. Hirota
Masahiro Niikura
S. F. Paul Man
Don D. Sin
IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
Respiratory Research
author_facet Kimia Shahangian
David A. Ngan
H. H. Rachel Chen
Yeni Oh
Anthony Tam
Jing Wen
Chung Cheung
Darryl A. Knight
Delbert R. Dorscheid
Tillie L. Hackett
Michael R. Hughes
Kelly M. McNagny
Jeremy A. Hirota
Masahiro Niikura
S. F. Paul Man
Don D. Sin
author_sort Kimia Shahangian
title IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
title_short IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
title_full IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
title_fullStr IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
title_full_unstemmed IL-4Rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
title_sort il-4rα blockade reduces influenza-associated morbidity in a murine model of allergic asthma
publisher BMC
series Respiratory Research
issn 1465-993X
publishDate 2021-03-01
description Abstract Background Asthma was identified as the most common comorbidity in hospitalized patients during the 2009 H1N1 influenza pandemic. We determined using a murine model of allergic asthma whether these mice experienced increased morbidity from pandemic H1N1 (pH1N1) viral infection and whether blockade of interleukin-4 receptor α (IL-4Rα), a critical mediator of Th2 signalling, improved their outcomes. Methods Male BALB/c mice were intranasally sensitized with house dust mite antigen (Der p 1) for 2 weeks; the mice were then inoculated intranasally with a single dose of pandemic H1N1 (pH1N1). The mice were administered intraperitoneally anti-IL-4Rα through either a prophylactic or a therapeutic treatment strategy. Results Infection with pH1N1 of mice sensitized to house dust mite (HDM) led to a 24% loss in weight by day 7 of infection (versus 14% in non-sensitized mice; p < .05). This was accompanied by increased viral load in the airways and a dampened anti-viral host responses to the infection. Treatment of HDM sensitized mice with a monoclonal antibody against IL-4Rα prior to or following pH1N1 infection prevented the excess weight loss, reduced the viral load in the lungs and ameliorated airway eosinophilia and systemic inflammation related to the pH1N1 infection. Conclusion Together, these data implicate allergic asthma as a significant risk factor for H1N1-related morbidity and reveal a potential therapeutic role for IL-4Rα signalling blockade in reducing the severity of influenza infection in those with allergic airway disease.
url https://doi.org/10.1186/s12931-021-01669-0
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